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174603-49-7 | 6-CHLORO-4-FLUORO-1-INDANONE

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Purchase CAS:174603-49-7 | 6-CHLORO-4-FLUORO-1-INDANONE,view related peer-reviewed papers,technical documents,similar products,MSDS & more.6-Chloro-4-fluoro-2,3-dihydro-1H-inden-1-one is a chemical compound with the molecular formula C9H6ClFO . It is a derivative of 1H-Inden-1-one, which is a bicyclic compound consisting of a benzene ring fused to a cyclopentene ....
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CAS:174603-49-7 | 6-CHLORO-4-FLUORO-1-INDANONE,Description

6-Chloro-4-fluoro-2,3-dihydro-1H-inden-1-one is a chemical compound with the molecular formula C9H6ClFO. It is a derivative of 1H-Inden-1-one, which is a bicyclic compound consisting of a benzene ring fused to a cyclopentene.

 

Synthesis Analysis

The synthesis of indanone derivatives, such as 6-Chloro-4-fluoro-2,3-dihydro-1H-inden-1-one, involves various methods. One common method is the cyclization of electron-rich 2-alkyl-1-ethynylbenzene derivatives. Other methods include the palladium-catalyzed carbonylative cyclization of unsaturated aryl iodides and dienyl triflates, iodides, and bromides.

 

Scientific Research Applications

 

Application 1: Antibacterial and Antifungal Studies

  • Summary of the Application: 2,3-dihydro-1H-inden-1-one derivatives have been synthesized and studied for their antibacterial and antifungal properties.
  • Methods of Application: A total of 15 derivatives from 2,3-dihydro-1H-inden-1-one were synthesized by grinding, stirring, and ultrasound irradiation methods.
  • Results: The synthesized compounds were tested against two Gram-positive (Staphylococcus aureus and Bacillus subtilis) and two Gram-negative bacteria (Escherichia coli and Proteus vulgaris), and also two fungal agents (Aspergillus niger and Candida albicans). Most of the compounds were found to exert potent antibacterial action with broad-spectrum antibacterial activity.

Application 2: Antileishmanial Evaluation

  • Summary of the Application: 2,3-dihydro-1H-pyrrolo[3,4-b]quinolin-1-one derivatives, which are similar to 2,3-dihydro-1H-inden-1-one, have been evaluated for their antileishmanial activity.
  • Methods of Application: The specific methods of application or experimental procedures were not detailed in the source.
  • Results: In vivo antileishmanial evaluation of one of the derivatives demonstrated 56.2% inhibition in liver and 61.1% inhibition in spleen parasite burden in infected Balb/c mice.

Application 3: Antiviral Activity

  • Summary of the Application: Indole derivatives, such as 6-Amino-4-substitutedalkyl-1H-indole-2-substitutedcarboxylate, have been reported as potential antiviral agents.
  • Methods of Application: The specific methods of application or experimental procedures were not detailed in the source.
  • Results: Compound methyl 6-amino-4-isobutoxy-1H-indole-2-carboxylate showed inhibitory activity against influenza A with IC50 = 7.53 μmol/L and the highest selectivity index (SI) value 17.1 to CoxB3 virus.

Application 4: Anticancer Activity

  • Summary of the Application: Indole derivatives have been found to possess anticancer activity.
  • Methods of Application: The specific methods of application or experimental procedures were not detailed in the source.
  • Results: The results of the anticancer activity of indole derivatives were not detailed in the source.

Application 5: Antimalarial Activity 

  • Summary of the Application: Quinoline derivatives, which are structurally similar to indole, have been used for a long time as a basic structure for the search of synthetic antimalarial drugs.
  • Methods of Application: The specific methods of application or experimental procedures were not detailed in the source.
  • Results: The results of the antimalarial activity of quinoline derivatives were not detailed in the source.

Application 6: Antihypertensive Activity

  • Summary of the Application: Imidazole derivatives, which are structurally similar to indole, have been reported to show antihypertensive activity.
  • Methods of Application: The specific methods of application or experimental procedures were not detailed in the source.
  • Results: The results of the antihypertensive activity of imidazole derivatives were not detailed in the source.

Application 7: Antiobesity Activity

  • Summary of the Application: Imidazole derivatives have also been reported to show antiobesity activity.
  • Methods of Application: The specific methods of application or experimental procedures were not detailed in the source.
  • Results: The results of the antiobesity activity of imidazole derivatives were not detailed in the source.

Safety And Hazards

The safety data sheet for 6-Chloro-4-fluoro-2,3-dihydro-1H-inden-1-one indicates that it may be harmful if swallowed, causes skin and eye irritation, and may cause respiratory irritation. The signal word for this compound is "Warning".

More Information

Product Name:6-CHLORO-4-FLUORO-1-INDANONE
Synonyms:6-CHLORO-4-FLUORO-1-INDANONE;6-CHLORO-4-FLUORO-INDAN-1-ONE;6-CHLORO-4-FLUORO-2,3-DIHYDRO-1H-INDEN-1-ONE;6-Chloro-4-flouro-1-indanone;6-chloro-4-fluoro-2,3-dihydroinden-1-one;1H-Inden-1-one, 6-chloro-4-fluoro-2,3-dihydro-
CAS:174603-49-7
MF:C9H6ClFO
MW:184.59
EINECS: 
Product Categories: 
Mol File:174603-49-7.mol
 
6-CHLORO-4-FLUORO-1-INDANONE Chemical Properties
storage temp. Sealed in dry,Room Temperature

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MS

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1HNMR

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CNMR

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IR1

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IR2

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Raman


 

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